Implant for Augmentation of Cerebral Blood Flow Trial-1 (ImpACT-1). A single-arm feasibility study evaluating the safety and potential benefit of the Ischemic Stroke System for treatment of acute ischemic stroke

• Published in: PloS one Vol. 14; no. 7; p. e0217472
• Main Authors: Khurana, Dheeraj, Kaul, Subhash, Schneider, Dietmar, Csanyi, Attila, Adam, Ilona, Ichaporia, Nasli R, Griewing, Bernd, Csiba, Laszlo, Valikovics, Attila, Puri, Vinod, Diener, Hans Christoph, Schwab, Stefan, Hetzel, Andreas, Bornstein, Natan
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 03-07-2019; Public Library of Science (PLoS)
• Subjects: Adolescent; Adult; Aged; Aged, 80 and over; Analysis; Animal models; Biology and Life Sciences; Blood; Blood circulation; Blood flow; Blood Flow Velocity; Blood-brain barrier; Brain; Brain Ischemia - physiopathology; Brain Ischemia - therapy; Care and treatment; Cerebral blood flow; Cerebrovascular Circulation; Clinical trials; Electric Stimulation Therapy; Engineering and Technology; Feasibility Studies; Female; Follow-Up Studies; Ganglia, Parasympathetic - physiopathology; Ganglion cysts; Hospital patients; Humans; Implantation; Ischemia; Male; Medical research; Medicine and Health Sciences; Middle Aged; Mortality; Parasympathetic nervous system; Patients; Research and Analysis Methods; Safety; Stimulation; Stroke; Stroke - physiopathology; Stroke - therapy; Teaching hospitals; Veins & arteries; Israel; Hungary; Tel Aviv Israel; Germany; India
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0217472

The Ischemic Stroke System is a novel device designed to deliver stimulation to the sphenopalatine ganglion(SPG).The SPG sends parasympathetic innervations to the anterior cerebral circulation. In rat stroke models, SPG stimulation results in increased cerebral blood flow, reduced infarct volume, protects the blood brain barrier, and improved neurological outcome. We present here the results of a prospective, multinational, single-arm, feasibility study designed to assess the safety, tolerability, and potential benefit of SPG stimulation inpatients with acute ischemic stroke(AIS).
Patients with anterior AIS, baseline NIHSS 7-20 and ability to initiate treatment within 24h from stroke onset, were implanted and treated with the SPG stimulation. Patients were followed up for 90 days. Effect was assessed by comparing the patient outcome to a matched population from the NINDS rt-PA trial placebo patients.
Ninety-eight patients were enrolled (mean age 57years, mean baseline NIHSS 12 and mean treatment time from stroke onset 19h). The observed mortality rate(12.2%), serious adverse events (SAE)incidence(23.5%) and nature of SAE were within the expected range for the population. The modified intention to treat cohort consisted of 84 patients who were compared to matched patients from the NINDS placebo arm. Patients treated with SPG stimulation had an average mRS lower by 0.76 than the historical controls(CMH test p = 0.001).
The implantation procedure and the SPG stimulation, initiated within 24hr from stroke onset, are feasible, safe, and tolerable. The results call for a follow-up randomized trial (funded by BrainsGate; clinicaltrials.gov number, NCT03733236).